KR20170106656A - Azeotrope-like compositions of cis-1,1,1,4,4,4-hexafluoro-2-butene - Google Patents

Abstract

를 갖는 cis-1,1,1,4,4,4-헥사플루오로-2-부텐(Z-HFO-1336mzzm) 화합물; 및 물, 플루오로케톤, 알코올, 하이드로클로로플루오로올레핀 및 이들의 둘 이상의 조합으로 이루어진 군으로부터 선택되는 다른 물질을 유효량으로 포함하는 공비성 조성물의 사용에 관한 것이다. 이러한 조성물은 발포제, 냉매, 가열제, 동력 사이클제(power cycle agent), 세정제, 에어로졸 추진제, 살균제, 윤활제, 맛과 향기 추출용매, 인화성 감소제, 및 인화 억제제와 같은 다양한 적용에 사용될 수 있다.The present invention relates to azeotropic compositions, methods and systems having utility in a variety of applications,

1,1,1,4,4,4-hexafluoro-2-butene (Z-HFO-1336mzzm) compound having the formula: And other materials selected from the group consisting of water, fluoroketones, alcohols, hydrochlorofluoroolefins, and combinations of two or more thereof. Such compositions can be used in a variety of applications such as foaming agents, refrigerants, heating agents, power cycle agents, detergents, aerosol propellants, bactericides, lubricants, flavor and aroma extraction solvents, flammability reducing agents, and flame retardants.

Description

Azeotropic compositions of CIS-1,1,1,4,4,4-hexafluoro-2-butene {AZEOTROPE-LIKE COMPOSITIONS OF CIS-1,1,1,4,4,4-HEXAFLUORO-2-BUTENE }

[Cross reference of related application]

This application claims priority to U.S. Provisional Application No. 61 / 287,041, filed December 16, 2009, which is incorporated herein by reference.

[TECHNICAL FIELD]

The present invention relates to azeotropic compositions, methods and systems having utility in a variety of applications,

1,1,1,4,4,4-hexafluoro-2-butene (Z-HFO-1336mzzm) compound having the formula: And other materials selected from the group consisting of water, fluoroketones, alcohols, hydrochlorofluoroolefins, and combinations of two or more thereof. The present invention also relates to the use of an azeotropic composition comprising, or consist essentially of, an effective amount.

The azeotropic compositions of the present invention are part of a continuing search of low global warming potential materials for the next generation. Such materials must have a low environmental impact, as measured by an extremely low global warming index and an ozone depletion potential near zero.

The azeotropic composition of the present invention can be used as a blowing agent, a refrigerant, a heating agent, a power cycle agent, a detergent, an aerosol propellant, a disinfectant, a lubricant, a flavor and fragrance extracting solvent, And may be used in various applications such as a photoresist inhibitor.

Applicants have developed several azeotropic compositions containing Z-HFO-1336mzzm as an essential component. In certain embodiments, the other portion of the azeotropic composition is at least one C1 to C12 alcohol compound. In another embodiment, the other part of the azeotropic composition is water. In another embodiment, another portion of the azeotropic composition is a fluoroketone compound. In another embodiment, another portion of the azeotropic composition is a hydrochlorofluoroolefin compound.

According to certain embodiments, the present invention provides a pharmaceutical composition comprising greater than 0 to about 99 wt% Z-HFO-1336mzzm compound; And from about 1% to less than 100% by weight of an alcohol, and combinations of two or more thereof, or preferably consist essentially of the composition. Preferred alcohols are C1 to C12 alcohols. Methanol and ethanol are particularly preferred.

It should be noted that products designated as Z-HFO-1336mzzm include in particular E-HFO-1336mzzm and are generally predicted to contain a small percentage, for example from about 0.5% to about 5% by weight, . As used herein, the term "consisting essentially of Z-HFO-1336mzzm" is intended to include the composition in general. As used herein, the terms "comprise" and "comprise" do not include other components. All embodiments of the invention described herein can be obtained in a substantially refined form, if desired, such that the embodiment is preferably composed of only the actual ingredients specified, other than the small (e.g., ppm) impurities.

The present invention preferably provides azeotropic and azeotropic compositions comprising, preferably consisting essentially of, Z-HFO-1336mzzm / ethanol or Z-HFO-1336mzzm / methanol. Preferably, the azeotropic composition of the present invention comprises, or more preferably comprises, an effective amount of Z-HFO-1336mzzm and ethanol or Z-HFO-1336mzzm and methanol. As used herein, the term "effective amount" refers to the amount of each component when combined with other components or components that will form the current azeotropic composition.

In certain embodiments, the azeotropic composition comprises from about 75% to less than 100% by weight of Z-HFO-1336mzzm and from greater than 0 to about 25% by weight of alcohol, and combinations of two or more thereof, .

In another embodiment, the azeotropic composition comprises from about 85% to less than 100% by weight of Z-HFO-1336mzzm and from greater than 0 to about 15% by weight of alcohol, and combinations of two or more thereof, .

Another embodiment of the present invention is directed to an azeotropic composition comprising greater than 0 to about 99 wt% water and about 1 wt% to less than 100 wt% Z-HFO-1336mzzm.

In certain embodiments, the azeotropic composition comprises, preferably consists essentially of, from greater than 0 to about 50% by weight of water and from about 50% to less than 100% by weight of Z-HFO-1336mzzm.

In another embodiment, the azeotropic composition comprises, preferably consists essentially of, from greater than 0 to about 10% by weight of water and from about 90% to less than 100% by weight of Z-HFO-1336mzzm.

One embodiment of the present invention is a blowing agent comprising, or consist essentially of, one or more azeotropic compositions of the present invention.

Another embodiment of the present invention is a method of forming a foam comprising the step of adding a foamable composition comprising a blowing agent, comprising or essentially consisting of one or more azeotropic compositions of the present invention. The blowing agent comprises a premix of polyol and blowing agent, and the blowing agent comprises the azeotropic composition of the present invention.

Another embodiment of the present invention is a closed cell foam provided by a foamable composition in the presence of a blowing agent comprising or essentially consisting of one or more azeotropic compositions of the present invention. Preferably, the closed cell foam is formed from a foamable composition further comprising a polyurethane, polyisocyanurate, polystyrene, polyethylene, and mixtures thereof.

One embodiment of the present invention is a refrigerant composition comprising or essentially consisting of one or more azeotropic compositions of the present invention. Another embodiment of the present invention is a cooling system comprising a refrigerant composition of the present invention. Yet another embodiment of the present invention is a method of cooling an article comprising the step of evaporating the refrigerant composition of the present invention in the vicinity of the article to be cooled.

Another embodiment of the present invention is a method of heating an article comprising condensing a refrigerant composition comprising or essentially consisting of one or more azeotropic compositions of the present invention in the vicinity of the article to be heated.

One embodiment of the invention is an injectable composition comprising a propellant and an injected material comprising or essentially consisting of one or more azeotropic compositions of the present invention.

Another embodiment of the present invention is a method of reducing the flammability of a fluid comprising adding to the fluid one or more azeotropic compositions of the present invention.

Another embodiment of the present invention is a method of inhibiting a print comprising contacting a flame with a fluid comprising one or more azeotropic compositions of the present invention. Optionally, such fluids may further comprise one or more fluoroketone compounds. One preferred fluoroketone compound is dodecafluoro-2-methylpentan-3-one. One source for this compound is Novec 1230 from 3M Corporation.

Another embodiment of the present invention is a method of cleaning and / or disinfecting an article comprising contacting the article to be cleaned or sterilized with a composition comprising or essentially consisting of one or more azeotropic compositions of the present invention . Optionally, the composition may further comprise ethylene oxide.

AZEOTROPE-LIKE

The term azeotrope-like means a composition that behaves like an azeotropic mixture, i.e., the composition of the vapor formed during boiling or evaporation is the same or substantially the same as the original liquid composition. Thus, while boiling or evaporating, the liquid composition changes to a minimum or negligible extent even if changed. This is in contrast to a non-azeotropic composition in which the liquid composition changes to a substantial degree during boiling or evaporation.

Thus, the term "azeotropic" is intended to be used in a broad sense including both compositions in strict sense and compositions acting as azeotropic mixtures. According to the basic law, the thermodynamic state of a fluid is defined as pressure, temperature, liquid composition and vapor composition. An azeotropic mixture is a system of two or more components with the same liquid composition and vapor composition in a system at a given pressure and temperature. In particular, this means that the components of the azeotropic mixture have a constant boiling point and can not be separated during the phase change.

In particular, the term "azeotropic" means that one or more compounds that behave substantially as a single compound and a Z-HFO-1336mzzm compound that behaves like a substantially single compound, as long as the vapor in substantial equilibrium with the liquid has substantially the same concentration as the component present in the liquid ≪ / RTI >

The azeotropic compositions according to the present invention can be prepared by reacting an azeotropic composition according to the invention with a complete azeotropic composition (a composition that satisfies an azeotropic condition at a specific pressure above a certain temperature value (maximum critical step)) or a limited azeotropic composition (a composition that satisfies an azeotropic condition only at a specific temperature in a specific temperature range) . In addition, the azeotropic compositions according to the present invention comprise single-azeotrope (the composition is present in a single liquid phase at a given pressure) or hetero-azo (the composition is present in more than one liquid phase at a given pressure). Further, the azeotropic composition according to the present invention may have a secondary, tertiary, quaternary, or pentavalent azeotropic mixture depending on whether the composition is composed of two, three, four, or five (or more) Lt; / RTI >

The azeotropic composition of the present invention may include additional components that do not form a new azeotropic system or additional components that are not present in the first distillation cut. The first distillation cut was the first cut obtained after the distillation column showed steady state operation under the total reflux condition. One way in which the addition of components determines whether a new azeotropic system is to be formed besides the present invention is to distill a sample of the composition as a component under conditions that are expected to separate the non-azeotropic mixture into its respective components. When the mixture containing the additional ingredients is non-azeotropic, the additional ingredients will be fractionally distilled from the azeotropic composition. When the mixture is azeotropic, some limited amount of first distillation cuts having a constant boiling point or containing all the mixed components acting as a single material will be obtained.

Another feature of the azeotropic composition is that there is a range of compositions containing varying proportions of the same composition having an azeotropic or constant boiling point. As used herein, "constant boiling" means that the boiling point of the composition is only about +/- 2 DEG C, preferably only about +/- 1 DEG C, more preferably only about < RTI ID = ± 0.5 ° C and most preferably only about ± 0.2 ° C. All such compositions are intended to be included within the terms "azeotropic" and "constant boiling point ". For example, at different pressures, the composition of a given azeotropic composition will vary at least slightly, since the boiling point of the composition is at least slightly different.

As described above, the azeotropic composition of the present invention has a constant boiling point or an essentially constant boiling point. In other words, for this azeotropic composition, the composition of the vapor formed during boiling or evaporation is the same as, or substantially the same as, the original liquid composition. Thus, while boiling or evaporating, the liquid composition varies only to a minimum or negligible extent as it varies. This is in contrast to non-azeotropic compositions in which the liquid composition changes to a substantial degree during boiling or evaporation.

Thus, the compositions of component A and component B exhibit a particular type of relationship, but are compositions which vary with temperature and / or pressure. For azeotropic compositions, there is a range of compositions containing varying proportions of the same components that are azeotropic. All such compositions are intended to be included in the term azeotropic as used herein.

Preferred azeotropic compositions of the present invention are environmentally acceptable and do not contribute to depletion of the ozone layer outside the Earth's atmosphere. The compounds and compositions of the present invention have no substantial ozone depletion potential (ODP), preferably no ODP greater than about 0.5, more preferably no greater than about 0.25, and most preferably, Has an ODP not greater than about 0.1; And / or a global warming potential (GWP) not greater than about 150, and more preferably no greater than about 50 GWP. Preferably, the composition meets both criteria.

As used herein, ODP is defined in the World Meteorological Association report, "Scientific Assessment of Ozone Depletion, 2002 ", which is incorporated herein by reference.

As used herein, GWP is defined in terms of the exponent of carbon dioxide and the horizon for a period of 100 years and is defined in the same reference as for ODP described above.

In one preferred embodiment, the present invention provides an azeotropic composition comprising, or preferably consisting essentially of, Z-HFO-1336mzzm and ethanol. Another preferred embodiment of the present invention provides an azeotropic composition comprising, preferably consisting essentially of, Z-HFO-1336mzzm and methanol. Other alcohols such as propanol, butanol, pentanol, hexanol, octanol, nonanol, decanol and the like can similarly be used.

Figure 1 shows the k-factor of the polyurethane foam.

In an azeotropic composition of the present invention, the amount of Z-HFO-1336mzzm can vary widely and in all cases comprises constituting the balance of the composition after occupying all the other components in the composition.

As noted above, methanol and ethanol are preferred alcohols used in preferred azeotropic compositions of the present invention. Preferably, this embodiment comprises from greater than 0 to about 50 parts by weight of ethanol and from about 50 parts by weight to less than about 100 parts by weight of Z-HFO-1336mzzm, more preferably from greater than 0 to about 20 parts by weight of ethanol and from about 80 parts to about Less than 100 parts by weight of Z-HFO-1336mzzm, more preferably more than 0 parts by weight of ethanol and from about 90 parts by weight to less than 100 parts by weight of Z-HFO-1336mzzm, preferably consisting essentially of ≪ / RTI > A preferred ethanol-based azeotropic composition of the present invention is characterized by having a boiling point of 14.3 psia, about 31.3 캜, preferably 賊 2 캜, more preferably 賊 1 캜.

Preferably, this embodiment comprises from about 1 part by weight to about 50 parts by weight of methanol and from about 50 parts by weight to about 99 parts by weight of Z-HFO-1336mzzm, more preferably from about 1 part by weight to about 70 parts by weight of methanol, More preferably from about 1 part by weight to about 85 parts by weight of methanol and from about 15 parts by weight to about 99 parts by weight of Z-HFO-1336mzzm, preferably from about 1 part by weight to about 99 parts by weight of Z-HFO-1336mzzm, Lt; RTI ID = 0.0 > azeotropic < / RTI > A preferred composition of the present invention is characterized by having a boiling point of 14.3 psia, about 29.7 캜, preferably 賊 2 캜, more preferably 賊 1 캜.

If desired, additional ingredients may be added to tailor the characteristics of the azeotropic composition of the present invention. By way of example, when the azeotropic composition of the present invention is used as a refrigerant, an oil solubility aid may be added. In addition, stabilizers and other materials may be added to enhance the properties of the azeotropic composition of the present invention.

Using an extraction solvent such as water, ethanol or methanol can be removed from the azeotrope. Because of the high solubility of each alcohol in water, the alcohol will be removed in aqueous solution and Z-HFO-1336mzzm is phase separated from the aqueous phase and remains as purified Z-HFO-1336mzzm. Then, using conventional drying techniques such as molecular sieves, the alcohol can be extracted from water.

Preferably, another embodiment comprises from about 1 part by weight to about 50 parts by weight of water and from about 50 parts by weight to 99 parts by weight of Z-HFO-1336mzzm, more preferably from about 10 parts by weight to about 40 parts by weight of water and from about 60 parts by weight Preferably from about 15 parts by weight to about 35 parts by weight of water and from about 65 parts by weight to 85 parts by weight of Z-HFO-1336mzzm, more preferably from about 15 parts by weight to about 85 parts by weight of Z-HFO-1336mzzm, ≪ / RTI > A preferred composition of the present invention is characterized by having a boiling point at 14.5 psia, about 31.4 占 폚, preferably 占 占 폚, more preferably 占 占 폚.

Preferably, another embodiment comprises about 1 part by weight to about 50 parts by weight of fluoro ketone dodecafluoro-2-methylpentan-3-one and about 50 parts by weight to 99 parts by weight of Z-HFO-1336mzzm, From about 5 parts by weight to about 45 parts by weight of Novec 1230 and from about 55 parts by weight to 95 parts by weight of Z-HFO-1336mzzm, even more preferably from about 10 parts by weight to about 30 parts by weight of fluoroketone, 90 parts by weight of Z-HFO-1336mzzm. ≪ / RTI > A preferred composition of the present invention is characterized by having a boiling point at 14.5 psia, of about 32.0 占 폚, preferably 占 폚, more preferably 占 占 폚.

The composition according to the invention comprises the preferred azeotropic composition and may comprise one or more components such as additives which do not form new azeotropic compositions. To tailor the composition for a particular application, additives known in the composition can be used. In addition, inhibitors may be added to the compositions to inhibit degradation, react with undesirable decomposition products, and / or prevent corrosion of metal surfaces. Generally, up to about 2 percent of the inhibitor may be used, based on the total weight of the azeotropic composition.

AZEOTROPE ADDITIVE

The azeotropic composition of the present invention may further comprise any of a variety of optional additives including stabilizers, metal passivators, corrosion inhibitors, and the like.

According to certain embodiments, the azeotropic composition of the present invention further comprises a stabilizer. Any of a variety of compounds suitable for stabilizing the azeotropic composition of the present invention may be used. Examples of certain preferred stabilizers include stabilizer compositions comprising at least one epoxide selected from the group consisting of aromatic epoxides, alkyl epoxides, alkenyl epoxides, and combinations of two or more thereof, and at least one phenolic composition . The stabilizer mixture may further comprise nitromethane, 1,2-butylene oxide and 1,3-dioxolane or 1,4-dioxane. In addition, mineral spirits, glycol ethers, alcohols and ketones, as well as terpene hydrocarbons and terpene alcohols can be used with the stabilizer mixtures given above.

Any of a variety of phenolic compounds are suitable for use in the present compositions. Applicants do not wish to be bound by any theory of operation or to the theory, but phenol acts as a radical scavenger in the azeotropic composition, thereby increasing the stability of the composition. As used herein, the term phenolic compound generally refers to any phenol that is substituted or unsubstituted. Examples of suitable phenolic compounds are 2,6-di-tert-butyl-4-methylphenol, 2,6-di-tert- ≪ RTI ID = 0.0 > alkylated < / RTI > alkylated hydroquinone and hydroquinone including tert-butylhydroquinone, other derivatives of hydroquinone and the like; Butylphenol), 4,4'-thiobis (2-methyl-6-tert-butylphenol), 4,4'- Methyl-6-tert-butylphenol) and the like; (2,6-di-tert-butylphenol), 4,4'-bis (2,6-di-tert-butylphenol), 2,2- (4-methyl-6-tert-butylphenol), 4,4-butylidenebis (3-methyl- (2,6-di-tert-butylphenol), 2,2'-methylenebis (4-methyl-6-nonylphenol), 2,2'-isobutylidenebis - dimethylphenol), alkylidene-bisphenols including 2,2'-methylenebis (4-methyl-6-cyclohexylphenol); 2,2-biphenyldiol or 4,4-biphenyldiol containing 2,2'-methylenebis (4-ethyl-6-tert-butylphenol); Butylated hydroxytoluene (BHT); (6-tert-butyl-m-cresol), acrylic aminophenol, 2,6-di-tert-butyl- Bis (3,5-di-tert-butyl-4-hydroxyphenyl) sulfide, 4- (N, N'-dimethylaminomethylphenol) Benzyl) sulfide, and the like, as well as phenolic UV absorbers and light stabilizers, as well as phenols containing at least one substituted or unsubstituted cyclic, linear, or branched aliphatic substituent, such as bisphenols containing heteroatoms including sulfides, .

Certain preferred phenols include alkylated monophenols such as tocopherol, BHT, hydroquinone, and the like. Particularly preferred phenols include tocopherol and the like. Most phenols are commercially available. Mixtures of single phenolic compounds and / or two or more phenols may be used in the present compositions. Any of a variety of epoxides will be suitable for use in the azeotropic compositions of the present invention. Applicants do not wish to be bound by any theory or any theory of operation, but the epoxide of the present invention acts as an acid scavenger in the azeotropic composition, thereby increasing the stability of the composition. Mixtures of single aromatic epoxides and / or two or more aromatic epoxides may be used in the present compositions.

In another specific preferred embodiment, the alkyl epoxide used as the acid scavenger of the present composition comprises polypropylene glycol diglycidyl ether. Examples of polypropylene glycol diglycidyl ethers suitable for use in the present invention include ethers available from SACHEM (Europe).

Also, in certain embodiments, the epoxide used in the present invention comprises two or more combinations of aromatic, alkyl and / or alkenyl substituents. Generally, such epoxides are referred to as "multisubstituted epoxides ". According to certain preferred embodiments, the stabilizer used in the present invention comprises a combination of at least one phenolic compound and at least one aromatic, alkyl or alkenyl epoxide. Examples of suitable combinations include tocopherol and allyl glycidyl ether, stabilizers including BHT and glycidyl butyl ether, and the like. Certain particularly preferred combinations include stabilizers including tocopherol and allyl glycidyl ether and the like.

Any suitable relative amount of at least one phenolic compound and at least one aromatic, alkyl or alkenyl epoxide may be used in the preferred stabilizer. For example, the weight ratio of the phenolic compound to the aromatic or fluorinated alkyl epoxide may vary from about 1: 99 to about 99: 1. In certain preferred embodiments, the weight ratio of the phenolic compound to the aromatic, alkyl, alkenyl, polydubstituted or fluorinated alkyl epoxide is about 30: 1, more preferably about 7: 1, more preferably about 2: 1 More preferably about 1: 1.

AZEOTROPE EXAMPLE

Example 1

Samples of 69.4 wt.% Z-HFO-1336mzzm, 3.1 wt.% Ethanol, 7.6 wt.% Light and rest of heavies were charged to a Monel distillation column. The distillation column is a spinning band column operated at atmospheric pressure. The condenser was cooled using a temperature-controlled propylene glycol aqueous solution.

First, the distillation column was operated at full reflux and allowed to reach temperature and pressure equilibrium at each desired condition. When the column was equilibrated, a vapor sample was taken from the overhead of the distillation column. The overhead of the column was periodically sampled while collecting the distillate. After removing light from the distillation column, a sample was taken. The sample showed 2.0 wt% ethanol in Z-HFO-1336mzzm. Ethanol present through Z-HFO-1336mzzm indicates that azeotrope is formed.

Example 2

An ebulliometer was used to measure the azeotrope of Z-HFO-1336mzzm and ethanol. The boiling system consists of a vacuum insulated glass vessel which is sealed at the bottom and open to the atmosphere from the top. The upper part or condenser part of the boiling system is surrounded by dry ice to ensure that all the vapor is condensed and can flow back into the boiling system. First, the boiling system is charged with Z-HFO-1336mzzm and ethanol is added.

Table 1 shows the minimum temperature at which an azimuth was formed. The bubble point temperature of the mixture remains constant, indicating that the mixture is azeotropic over a wide composition range.

Measurement of the boiling point of Z-HFO-1336mzzm and ethanol at 14.3 psia Z-HFO-1336mzzm,
weight% ethanol,
weight% Temperature,
℃ 100.00 0.00 31.6 99.59 0.41 31.3 97.97 2.03 31.2 95.65 4.35 31.1 93.43 6.57 31.1 89.95 10.05 31.1 84.30 15.70 31.2 79.32 20.68 31.3 74.90 25.10 31.3 70.53 29.47 31.3 66.64 33.36 31.4 63.15 36.85 31.4

Example 2

As in Example 2, a boiling system was used to determine the azeotrope of Z-HFO-1336mzzm and methanol. First, the boiling system was charged with Z-HFO-1336mzzm and methanol was added.

Table 2 shows the minimum temperature at which an azimuth was formed. The bubble point temperature of the mixture remains constant, indicating that the mixture is azeotropic over a wide composition range.

Measurement of the boiling point of Z-HFO-1336mzzm and methanol at 14.3 psia Z-HFO-1336mzzm,
weight% Methanol,
weight% Temperature,
℃ 100.00 0.00 32.02 99.59 0.41 30.81 98.78 1.22 29.92 97.20 2.80 29.68 94.19 5.81 29.66 91.35 8.65 29.66 86.17 13.83 29.78 81.55 18.45 29.80 77.39 22.61 29.90 73.19 26.81 29.94 69.43 30.57 29.99 66.03 33.97 30.14 62.96 37.04 30.24 60.15 39.85 30.44

Example 3

To determine the azeotrope of Z-HFO-1336mzzm and dodecafluoro-2-methylpentan-3-one (Novec 1230), the boiling system used in Example 2 was used. First, the boiling system was charged with Z-HFO-1336mzzm and a fluoroketone Novec 1230 (3M Company).

Table 3 shows the minimum temperature at which an azimuth is formed. The bubble point temperature of the mixture remains constant, indicating that the mixture is azeotropic over a wide composition range.

Measurement of the boiling point of Z-HFO-1336mzzm and Novec 1230 at 14.5 psia Z-HFO-1336mzzm, wt% NOVEC 1230,
weight% Temperature,
℃ 100.00 0.00 32.7 99.25 0.75 32.6 97.77 2.23 32.4 94.95 5.05 32.2 89.78 10.22 32.0 82.99 17.01 32.0 75.39 24.61 32.1 69.06 30.94 32.1 63.72 36.28 32.2 58.61 41.39 32.4 54.27 45.73 32.5 50.52 49.48 32.7 47.26 52.74 32.8 44.39 55.61 33.0

Example 4

The compound E-HCFO-1233zd (trans-1,1,1-trifluoro-3-chloropropene) was also found to form an azeotropic composition with Z-HFO-1336mzzm. As shown in Table 4 below, the azeotropic properties of this composition were confirmed to continue up to about 10% by weight Z-HFO-1336mzzm. Such compositions are particularly useful for spray foam applications.

Boiling measurement of Z-HFO-1336mzzm and E-HCFO-1233zd at 14.5 psia / 1233zd (E) / 1336mzzm (Z) 1233zd (E)
weight% 1336mzzm (Z)
weight% Temperature
(° C) 100.00 0.00 17.70 99.60 0.40 17.70 98.82 1.18 17.73 97.28 2.72 17.75 95.79 4.21 17.81 92.95 7.05 17.89 87.74 12.26 18.02 83.64 16.36 18.18 79.39 20.61 18.37 75.56 24.44 18.56 72.08 27.92 18.76 68.91 31.09 18.98 65.66 34.34 19.18 62.70 37.30 19.36 59.99 40.01 19.54 57.88 42.12 19.58 42.93 57.07 20.90 35.54 64.46 21.81 25.80 74.20 23.22 15.66 84.34 25.13 4.67 95.33 30.44 0.18 99.82 32.79 0.00 100.00 32.81

Example 5

To determine the azeotropic ratio of Z-HFO-1336mzzm and water, a boiling system as in Example 2 was used. First, the boiling system was charged with Z-HFO-1336mzzm and water was added. Table 5 shows the minimum temperature at which an azimuth is formed. The bubble point temperature of the mixture remains constant, indicating that the mixture is azeotropic over a wide composition range.

Measurement of the boiling point of Z-HFO-1336mzzm and water at 14.5 psia Z-HFO-1336mzzm,
weight% water,
weight% Temperature
℃ 100.0 0.0 32.4 99.4 0.6 32.3 98.2 1.8 32.0 97.1 2.9 31.8 96.0 4.0 31.7 93.9 6.1 31.5 89.8 10.2 31.4 82.8 17.2 31.4 76.7 23.3 31.4 71.5 28.5 31.4 66.9 33.1 31.4 62.9 37.1 31.4 59.4 40.6 31.4

Azeotropic  Use of composition

As noted above, any azeotropic composition of the present invention can be used in a wide variety of applications as a replacement for compositions containing CFCs, and less preferred HCFCs.

In particular, Z-HFO-1336mzzm; And other materials selected from the group consisting of water, fluoroketones, alcohols, hydrochlorofluoroolefins, and combinations of two or more thereof, in an effective amount, or an essentially azeotropic composition is designated for some preferred use Which is useful as a foaming agent, a refrigerant, a heating agent, a power cycle agent, a detergent, an aerosol propellant, a bactericide, a lubricant, a flavor and fragrance extracting solvent, a flammability reducing agent, and a phosphor inhibitor. Each of these uses will be discussed in more detail below.

Blowing agent (BLOWING AGENT)

One embodiment of the present invention is directed to a blowing agent comprising one or more azeotropic compositions of the present invention. In another embodiment, the invention provides a foamable composition, preferably a polyurethane and polyisocyanurate foam composition, and a process for making the foam. In such foam embodiments, one or more azeotropic compositions are included as a blowing agent in the foamable composition, and preferably the composition is capable of reacting and firing under suitable conditions to form a foam or a cellular structure, as is well known in the art One or more additional components.

Preferably, the method comprises the steps of providing such a foamable composition; And reacting the foamable composition under conditions effective to obtain a foam, preferably a closed cell foam. The present invention also relates to a foam, preferably a packed cell foam, made from a polymeric foam formulation containing a blowing agent comprising an azeotropic composition of the present invention.

In certain embodiments, it is preferred that one or more of the following HFC isomers are used as the co-blowing agent in the azeotropic composition of the present invention.

1,1,1,2,2-pentafluoroethane (HFC-125)

1,1,2,2-tetrafluoroethane (HFC-134)

1,1,1,2-tetrafluoroethane (HFC-134a)

1,1-difluoroethane (HFC-152a)

1,1,1,2,3,3,3-heptafluoropropane (HFC-227ea)

1,1,1,3,3,3-hexafluoropropane (HFC-236fa)

1,1,1,3,3-pentafluoropropane (HFC-245fa) and

1,1,1,3,3-pentafluoropropane (HFC-365mfc)

The relative amounts of any additional co-blowing agents presented above, as well as any additional components that may be included in the azeotropic compositions of the present invention, can vary widely within the general broad scope of the present invention, depending on the particular application of the composition, All relative amounts are considered within the scope of this specification.

Foam (FOAM)

The present invention also relates to a process for the preparation of a polymeric foam comprising a foamed formulation comprising a foaming agent comprising Z-HFO-1336mzzm and one or more alcohols, preferably methanol or ethanol, Cell foams, open cell foams, rigid foams, flexible foams, complete skins, and the like. The Applicant believes that one advantage of the thermosetting foams, such as the foams according to the invention, in particular the polyurethane foams according to the invention, is that with regard to the thermosetting foam embodiment, particularly preferably under the low temperature conditions as shown in Fig. 1, Lt; RTI ID = 0.0 > a < / RTI > factor or lambda.

While the foams of the present invention, especially thermosetting foams, are contemplated to be of use in a wide variety of applications, in certain preferred embodiments, the present invention provides a method of making a refrigerator foam, freezer foam, refrigerator / freezer foam, panel foam, And an appliance foam according to the present invention, including an application.

In certain preferred embodiments, the foams produced in accordance with the present invention have a low ozone depletion index and low global warming index that are highly related to the preferred foaming agents of the present invention, as well as thermal insulation efficiencies (especially thermosetting foams), dimensional stability, , ≪ / RTI > aging of thermal insulation properties, and the like.

In certain highly preferred embodiments, the present invention provides a thermosetting foam comprising such a foam formed of a foam article, which allows the same foaming agent (or the commonly used foaming agent HFC-245fa) to be the same ≪ / RTI > and exhibit improved thermal conductivity with respect to the foam produced using the composition.

For use in accordance with the foam embodiments of the present invention, such as those described in Polyurethanes Chemistry and Technology, Volumes I and II, Saunders and Frisch, 1962, John Wiley and Sons, New York, NY, Any method well known in the art may be used or employed. In general, this preferred method comprises mixing a mixture of isocyanates, polyols or polyols comprising one or more compositions, a blowing agent or a mixture of blowing agents with another material such as a catalyst, a surfactant, optionally a phosphor inhibitor, a colorant or other additives , ≪ / RTI > polyurethane or polyisocyanurate foams.

It is convenient in many applications to provide the components for a polyurethane or polyisocyanurate foam as a pre-mixed formulation. Most commonly, the foam formulation is pre-mixed with the two components. The isocyanate, optionally the specific surfactant and blowing agent generally comprise a first component, referred to as component A, Polyol or polyol mixtures, surfactants, catalysts, blowing agents, flame retardants and other isocyanate active ingredients generally comprise a second component, referred to as component B. Thus, a hand mix, preferably a mechanical mix, for small quantities of manufacture, to form blocks, slabs, laminates, pour-in-placel panels and other items, spray applied foams, By mixing together both the A side component and the B side component by a machine mix technique, polyurethane or polyisocyanurate foams can be easily produced. Alternatively, other materials such as a phosphor inhibitor, a colorant, an auxiliary blowing agent and other polyols may be added to the mixing head or reaction site as a third stream. However, most conveniently, all of these are incorporated into one B component as described above.

In addition, thermoplastic foams may be prepared using the azeotropic compositions of the present invention. For example, to prepare rigid foams, conventional foam polyurethane and isocyanurate formulations may be mixed with the azeotropic composition in a conventional manner.

In addition, dispersants, cell stabilizers and surfactants may be included in the blowing agent mixture. Surfactants, in particular silicone oil, may be added to serve as a cell stabilizer. Some representative materials are polysiloxane polyoxyalkylene block copolymers sold under the trade names DC-193, B-8404, and L-5340 and generally described in U.S. Patent Nos. 2,834,748, 2,917,480, and 2,846,458. Other optional additives for the blowing agent mixture include tri (2-chloroethyl) phosphate, tri (2-chloropropyl) phosphate, tri (2,3-dibromopropyl) , Di-ammonium phosphate, various halogenated aromatic compounds, antimony oxide, aluminum trihydrate, polyvinyl chloride, and the like.

Generally, the amount of blowing agent present in the blended mixture used to form the foamable composition of the present invention is determined by the desired foam density of the final polyurethane or polyisocyanurate foam product. The fabricated polyurethane foam has a density of from about 0.5 pounds per cubic foot to about 40 pounds per cubic foot, preferably from about 1.0 pounds per cubic foot to about 20.0 pounds per cubic foot, most preferably about 1.5 pounds per cubic foot per cubic foot of rigid polyurethane foam, Cubic feet to about 6.0 pounds per cubic foot and may vary from about 1.0 pounds per cubic foot to about 4.0 pounds per cubic foot for the flexible foam. The density obtained is a function of various factors, including how many foaming agents or foaming agents are present in the A and / or B components or whether they were added when the foam was made.

Examples of foaming agents and foams

This example shows the performance of a blowing agent comprising Z-HFO-1336mzzm and an alcohol used in connection with the preparation of a polyurethane foam. Three separate blowing agents were provided for this example. The first blowing agent is HFC-245fa. The second blowing agent is Z-HFO-1336mzzm. The third blowing agent comprises an azeotropic composition comprising Z-HFO-1336mzzm at a concentration of about 98 weight percent of the total blowing agent and ethanol at a concentration of about 2 weight percent of the total blowing agent.

In each system, a foaming agent was added at substantially the same molar concentration to the polyol blend. Each foaming agent was then used to form a foam, and the k-factor of the foam was measured. The formulations used are shown in Table 6. A foam was prepared with a pour time of 3 seconds and a mix time of 8 seconds. The feed temperature was 50 ℉ polyol / 70 MD MDI.

Polyol master batch composition ingredient php Manich polyether polyol, OH 470 80.00 Aromatic polyester polyol 70.00 Diethyl glycol 10.00 Silicone surfactant 2.00 Dimethylethanolamine 3.20 Neutral chlorinated phosphate ester 20.00 water 2.00 all 187.20 Foam agent mall 0.698 Index (Index) 110

Table 7 below and Figure 1 show the k-factor performance for three blowing agents.

K factor of polyurethane foam 245fa Z-HFO-1336mzzm Z-HFO-1336mzzm + 2 wt% ethanol Temperature, ℉ k,
BTU / hr ft < ² > F Temperature, ℉ k,
BTU / hr ft < ² > F Temperature, ℉ k,
BTU / hr ft < ² > F 40 0.132 40 0.137 40 0.135 75 0.147 75 0.146 75 0.145 110 0.164 110 0.162 110 0.161

One unexpected result in this example is that a 98 wt% Z-HFO-1336mzzm and 2 wt% ethanol mixture has an improved low temperature k factor compared to the k-factor of the pure Z-HFO-1336mzzm blowing agent .

SPRAY FOAM

In the example of the sprayed foams, surprisingly, by the use of an azeotropic composition consisting essentially of 4% by weight of Z-HFO-1336mzzm and 96% by weight of 1233zd (E), there is a significant and unexpected positive effect on the thermal conductivity . Foams made with this blowing agent composition were slowly aged over the entire temperature range and had better thermal conductivity than foams made with a blowing agent containing only 1233zd (E).

METHOD AND SYSTEM

The azeotropic compositions of the present invention are also useful in connection with a variety of methods and systems, including use as a heat transfer fluid in systems and methods for heat transfer, such as refrigerants used in refrigeration, air conditioning and heat pump systems. The azeotropic compositions of the present invention are also useful in the use of systems and methods for producing aerosols, preferably comprising, or consisting of, an aerosol propellant in such systems and methods. Also included in certain aspects of the invention are methods of suppressing and inhibiting prints and methods of forming foams. Also, in a particular aspect, the present invention provides a method of removing a residue from an article, wherein the azeotropic composition of the present invention is used as a solvent component in such methods and systems.

HEAT TRANSFER METHOD

A preferred method of heat transfer generally includes providing the azeotropic composition of the present invention and allowing the heat to be transferred to or from the composition by phase change of the composition. For example, the method provides cooling by absorbing heat from the fluid or article, preferably by evaporating the refrigerant component around a body or fluid that is cooled to produce a vapor comprising the composition.

Preferably, the method further comprises compressing the refrigerant vapor, typically with a compressor or similar equivalent, to produce the vapor of the present composition at a relatively elevated pressure. Generally, the step of compressing the steam adds heat to the steam, thereby increasing the temperature of the high-pressure steam relatively. Preferably, the method includes removing at least some of the heat added by the evaporation and compression steps from the relatively hot, high pressure steam. In order to produce a relatively high pressure fluid comprising the composition of the present invention, the steam is under relatively high pressure conditions, but the heat removal step preferably includes condensing the high temperature, high pressure steam. This relatively high pressure fluid then has a small isenthalpic reduction in pressure to produce a relatively low temperature, low pressure fluid. In such an implementation, the refrigerant fluid at such a reduced temperature is then evaporated by heat transfer from the cooled body or fluid.

In another process embodiment of the present invention, the azeotropic composition of the present invention may be used in a heating method comprising condensing a refrigerant comprising or essentially consisting of the azeotropic composition of the present invention, around a body or fluid to be heated have. As described above, this method is often the opposite cycle to the refrigeration cycle described above.

REFRIGERANT COMPOSITION

The azeotropic compositions of the present invention may be employed for use with automotive air conditioning systems and devices, commercial refrigeration systems and devices, chillers, household refrigerators and freezers, general air conditioning systems, heat pumps, and the like.

Many conventional refrigeration systems are currently employed for use with conventional refrigerants, and the azeotropic compositions of the present invention are known to be employed for use in many such systems, without altering or altering the system. In many applications, the azeotropic composition of the present invention may provide advantages as a substitute for the system, which is currently based on refrigerants having a relatively low capacity. Also, in embodiments where it is desirable to use a lower capacity refrigerant of the present invention, for example, due to the efficiency of replacing a higher capacity refrigerant, this embodiment of the present composition provides a potential advantage.

Thus, in certain embodiments it is preferred to use an azeotropic composition comprising or essentially consisting of Z-HFO-1336mzzm and one or more alcohols as a replacement for conventional refrigerants such as HCFC-123 or HFC-134a Do. In certain applications, the refrigerant of the present invention allows for the beneficial use of potentially larger displacement compressors, thereby having better energy efficiency than other refrigerants such as HCFC-123 or HFC-134a. Thus, the refrigerant composition of the present invention provides the possibility of obtaining the competitive advantage of the energy unit for refrigerant replacement application.

Although the azeotropic composition of the present invention is contemplated to comprise components in varying amounts, the refrigerant composition of the present invention is preferably present in an amount of at least about 50% by weight, more preferably at least about 70% by weight, Z-HFO-1336mzzm. ≪ / RTI >

POWER CYCLE USE

A Rankine cycle system is known as a simple and reliable means of converting thermal energy into mechanical axial force. When generating low levels of thermal energy, organic working fluids are useful instead of water / steam. Water / steam systems operating at low levels of thermal energy (typically below 400)) will be associated with high volume and low pressure. In order to reduce the system size and maintain high efficiency, an organic working fluid having a boiling point near room temperature is employed. Such fluids have a high gas density, as compared to water at low operating temperatures, which allows for high capacity and favorable transport, and has heat transfer characteristics, resulting in high efficiency. In particular, there are many opportunities to use flammable working fluids such as toluene and pentane at industrial sites, when the industrial site already has a large amount of flammability at the site of the process or storage. Other fluids, such as CFC-113 or CFC-11, have been used where risks associated with the use of flammable working fluids, such as power generation in populated areas or near buildings, can not be recognized. These materials are non-flammable, but have an environmental risk due to their ozone depletion potential. Preferably, the organic working fluid is environmentally acceptable, non-flammable, has a low degree of toxicity and must operate at a constant pressure.

As used herein, the term "nonflammable" means that when measured by one of the standard flash point methods, e.g., ASTM-1310 "Flash point of liquids by tag open- Refers to compositions and compounds of the present invention which are not shown.

Organic Rankine cycle systems are often used to recover waste heat in industrial processes. In combined heat and power (cogeneration) applications, the waste heat is recovered from the combustion of the fuel used to drive the prime mover of the generator set, for example to heat the building or to heat the absorption quencher to provide cooling , To make hot water. In some cases, there is little or no demand for hot water. The most difficult cases are when the temperature conditions are variable and load matching is difficult by interfering with the efficient operation of the combined heat and power systems. In this case, it is more useful to convert the waste heat to an axial force using an organic Rankine cycle system. The axial force may be used, for example, to operate the pump or may be used to generate electricity. Using this approach, the overall system efficiency is higher and fuel utilization is greater. More power can be generated for the same fuel input, so that air emissions from fuel combustion can be reduced.

The process for producing the waste heat is at least one selected from the group consisting of a fuel cell, an internal combustion engine, an internal compression engine, an external combustion engine and a turbine. Other sources of waste heat include refinery, petrochemical plants, oil and gas pipelines, chemical industry, commercial buildings, hotels, shopping malls, supermarkets, bakeries, food processing industries, restaurants, paint curing ovens, kiln, wood kiln (drying), calcining operation, steel industry, glass industry, foundry, smelting, air-conditioning, refrigeration and central heating. See U.S. Patent No. 7,428,816, which is incorporated herein by reference.

One particular embodiment of the power cycle use of such compounds is a method of recovering waste heat in an organic Rankine cycle system wherein the working fluid comprises Z-HFO-1336mzzm and one or more alcohols, preferably methanol or ethanol, ≪ / RTI >

Power cycle example

This example shows the use of the azeotropic composition of the present invention for use as a Rankine power cycle composition.

Smith, J. M. et al., Introduction to Chemical Engineering Thermodynamics; According to the procedure described in McGraw-Hill (1996), the effects of various working fluids can be compared in an organic Rankine cycle. In this example, the conditions used in the organic Rankine cycle calculation are 75% pump efficiency, 80% expander efficiency, 190 ° C boiler temperature, 45 ° C condenser temperature, and 1000W boiler heat. The performance of a 95: 5 wt.% Z-HFO-1336mzzm: methanol mixture is compared to the commercially available fluid HFC-245fa (available from Honeywell). Under certain conditions, the thermal efficiencies of HFC-245fa and 95: 5 wt% Z-HFO-1336mzzm: methanol mixtures are 0.142 and 0.158, respectively. This indicates that a 95: 5 wt% Z-HFO-1336mzzm: methanol mixture in the power cycle is performed better than HFC-245fa.

CLEANING AND CONTAMINANT REMOVAL

The present invention also provides a method of removing contaminants from a product, part, component, substrate, or any other article, or portion thereof, by applying the inventive azeotropic composition to the article. For convenience's sake, the term "article" is used herein to refer to all such articles, booms, components, substrates, and the like, and is further intended to refer to any surface or portion thereof. In addition, the term "contaminant" is intended to refer to an unwanted material or material present in the article when such material is intentionally placed on the article. For example, in the manufacture of semiconductor devices, it is common to place a photoresist material on a substrate in order to form a mask for an etching operation and then remove the photoresist material from the substrate. As used herein, the term "contaminant" is intended to cover and include such photoresist material.

A preferred method of the present invention involves applying the composition to an article. While a number of different cleaning techniques are contemplated to employ the azeotropic composition of the present invention for superior benefit, it is considered particularly advantageous to use the compositions in connection with supercritical cleaning techniques. Supercritical rinsing is disclosed in U.S. Patent No. 6,589,355, assigned to the assignee of the present invention and incorporated herein by reference.

For supercritical cleaning applications, it is preferred in certain embodiments to include, in addition to the azeotropic composition of the present invention, other ingredients such as CO ₂ and other known ingredients used in connection with supercritical cleaning applications Do.

Also, in certain embodiments, it may be possible and desirable to use the present cleaning compositions in conjunction with particular sub-critical vapor degreasing and solvent cleaning methods.

Other cleaning embodiments of the present invention include contaminant components and contaminant removal from the vapor compression system when the system is manufactured and serviced. As used herein, the term "contaminant " refers to processing fluids, lubricants, particles, sludge, and / or other materials that are used in the manufacture of such systems or that are produced during use of the system. Generally, these contaminants include compounds such as alkylbenzenes, mineral oils, esters, polyalkylene glycols, polyvinyl ethers, and other compounds consisting primarily of carbon, hydrogen and oxygen. The azeotropic compositions of the present invention will be useful for this purpose.

Cleaning composition example

This example illustrates the use of the azeotropic composition of the present invention for use as a cleaning composition.

The azeotropic composition is prepared to contain 95% by weight of Z-HFO-1336mzzm and about 5% by weight of ethanol. Various stainless steel coupons are contaminated with mineral oil, rosin flux or other contaminants. These coupons are then absorbed into the solvent blend. The blend can remove oil in a short period of time. Coupons are visibly observed for cleanliness. Similar results are expected with other mixtures. Similar results are expected with silicone oil.

Propellant for sprayable composition (PROPELLANT FOR SPRAYABLE COMPOSITION)

In another embodiment, the azeotropic composition of the present invention may be used alone or as a propellant in a sprayable composition, with known propellants. The propellant composition comprises the azeotropic composition of the present invention, more preferably it consists essentially of the azeotropic composition of the present invention, and even more preferably consists of the azeotropic composition of the present invention. Active ingredients, solvents, and other materials that are sprayed with the inert ingredients may also be present in the injectable mixture. Preferably, the sprayable composition is an aerosol. Suitable active materials include, but are not limited to, lubricants; Pesticide; detergent; Beauty materials such as deodorant, perfume and hair spray; As well as medical materials such as skin coolants (sunlight burn treatment), local anesthetics and oral contraceptives.

The injectable composition comprises a propellant and an injectable material comprising the azeotropic composition of the present invention. In addition, inert components, solvents, and other materials may be present in the injectable mixture. Preferably, the sprayable composition is an aerosol. Suitable injectable materials include, but are not limited to, cosmetic ingredients such as deodorants, perfumes, hair sprays; Detergents and polishes, as well as medical materials such as anti-asthma and anti-seizure medications.

STERILIZATION

In particular, many articles, devices and materials for use in the medical field must be sterilized prior to use for health and safety reasons, such as the health and safety of patients and hospital personnel. The present invention provides a method of sterilization comprising contacting an article, device or material to be sterilized with an azeotropic composition of the present invention, optionally one or more additional disinfectants.

Although many bactericides are known in the art and are considered suitable for use in connection with the present invention, in certain preferred embodiments the bactericides include ethylene oxide, formaldehyde, hydrogen peroxide, chlorine dioxide, ozone, and combinations thereof . In certain embodiments, ethylene oxide is the preferred disinfectant. In view of the techniques contained herein, those skilled in the art will readily be able to determine the relative molar ratios of the fungicides to the compositions used with the fungicidal compositions and methods, and all such ranges are within the scope of this disclosure.

As is known to those skilled in the art, certain bactericides, such as ethylene oxide, are highly flammable components and, in order to reduce the flammability of the bactericidal composition to an acceptable level, the compounds according to the present invention are included in the composition in an effective amount do. The sterilization method of the present invention can be hot or pasteurized, and the present invention preferably involves the use of a compound or composition of the present invention in a substantially sealed chamber at a temperature of from about 250 ℉ to about 270.. Generally, the process can be completed in less than about 2 hours. However, some articles, such as plastic articles and electrical parts, can not withstand such high temperatures, requiring pasteurization.

Sterilization example

In the pasteurization method, the article to be sterilized is exposed to a fluid comprising the composition of the present invention at a temperature from about room temperature to about 200 ℉, more preferably from about room temperature to about 100..

Pasteurization of the present invention is an at least two-step process carried out in a substantially sealed, preferably air tight chamber. In the first step (sterilization step), the article to be cleaned and packaged in the gas-permeable bag is placed in the chamber.

The vacuum is then pulled, perhaps by placing the air with the vapor, and drawing air out of the chamber. In certain embodiments, it is desirable to inject the vapor into the chamber, preferably to obtain a relative humidity ranging from about 30% to about 70%. This humidity can maximize the germicidal effect of the germicide, which is introduced into the chamber after the desired relative humidity is obtained. After a sufficient time for the sterilizing agent to permeate the package and reach the gaps in the article, the sterilizing agent and the vapor are removed from the chamber.

In a preferred second step of the process (aeration step), the article is aerated to remove the bactericide residue. Removal of such residues is optional in the present invention when substantially non-toxic compounds are used, but is particularly important in the case of toxic fungicides. Typical aeration processes include air wash, continuous aeration, and a combination of both. Airwashing is a batch process, which generally involves emptying the chamber for a relatively short period of time, for example 12 minutes, and then introducing air into the chamber above atmospheric pressure.

As used herein, the term "non-toxic" is used herein to refer to an Anesthesiology, Vol. 14, pp. Of the present invention having an acute toxicity level that is substantially less than the toxic level of HFO-1223xd, preferably at least about 30 percent relative less than the toxic level of HFO-1223xd, as measured by the method disclosed in US Pat. Compounds and compositions.

This cycle is repeated any number of times until the desired removal of the bactericide is achieved. In general, the continuous aeration includes the steps of introducing air through the inlet at one side of the chamber and then applying a small amount of vacuum to the outlet to draw air through the outlet at the other side of the chamber. The two approaches are often combined. For example, a common approach involves performing an air wash and subsequent aeration cycles.

LUBRICANT

In certain preferred embodiments, the azeotropic composition of the present invention may further comprise a lubricant. Any of a variety of conventional lubricants may be used in the azeotropic composition of the present invention. When used in refrigerant systems, an important requirement of the lubricant is that there must be sufficient lubricant to return to the compressor of the system to smooth the compressor. Thus, the suitability of the lubricant for a particular system is determined by the refrigerant / lubricant properties and, in part, by the characteristics of the system used.

Examples of suitable lubricants include mineral oils, alkylbenzenes, polyol esters including polyalkylene glycols, PAG oils and the like. Mineral oils, including paraffin oil or naphthenic acid oil, are commercially available. Commercially available mineral oils include Witco LP 250 from Witco, Zerol 300 from Shrieve Chemical, Sunisco 3GS from Witco and Calumet R015 from Calumet. Commercially available esters include Neerypentyl glycol dipelaconate available as Emery 2917 (R) and Hatcol 2370. Other useful esters include phosphates, dibasic acid esters and fluoro esters. Preferred lubricants include polyalkylene glycols and esters. Certain more preferred lubricants include polyalkylene glycols.

EXTRACTION OF FLAVOR AND FRAGRANCE

The azeotropic compositions of the present invention also provide advantages when used to transport, extract or separate the desired material from the biomass. Such materials include, but are not limited to, oils that can be used as emulsifiable oils, fuels, pharmaceuticals, functional foods, and the like, such as taste and aroma.

Extraction example

For this purpose, the suitability of the azeotropic composition of the present invention is demonstrated by the test procedure, wherein a sample of Jasmone is placed in a glass tube surrounded by a heavy wall. A suitable amount of the azeotropic composition of the present invention is added to the glass tube. The tube is then frozen and sealed. Upon thawing of the tube, the mixture has one liquid phase containing Jasmone and an azeotropic composition, which may be used as part of an extractant, carrier or delivery system for flavor and fragrance formulations in aerosols and other formulations Lt; / RTI > In addition, the test establishes the potential as a flavor and fragrance extract containing plant material.

FLAMMABILITY REDUCTION METHOD

According to certain other preferred embodiments, the present invention provides a method for reducing flammability, the method comprising adding an azeotropic composition of the present invention to the fluid. In accordance with the present invention, the flammability associated with any of a wide variety of other flammable fluids can be reduced. For example, in accordance with the present invention, ethylene oxide (HFC-152a), including 1,1,1-trifluoroethane (HFC-143a), difluoromethane (HFC-32), propane, hexane, , Flammable hydrofluorocarbons, and fluids such as hydrocarbons can be reduced. For this purpose of the present invention, flammable fluids exhibit flammability ranges in air as measured through any standard conventional test method such as ASTM E-681 and the like.

In order to reduce the flammability of the fluid according to the present invention, any suitable amount of the present compounds or compositions may be added. As will be appreciated by those skilled in the art, the amount added will depend, at least in part, on the degree of flammability of the subject fluid and on the desirability of reducing its flammability. In certain preferred embodiments, the amount of compound or composition added to the flammable fluid is effective to provide substantially non-flammability to the final fluid.

Reduced Flammability Example

This example illustrates the use of the azeotropic composition of the present invention for reducing flammability of other compositions.

In an ASTM E681 apparatus at ambient conditions, an azeotropic mixture of 97: 2 wt.% Z-HFO-1336mzzm: ethanol and isopentane vapor were mixed to yield a more 97: 2 wt.% Of Z-HFO-1336mzzm: ethanol The lower flammability limit (LFL) increases when an azeotropic mixture is added. This represents a lower flammability to the blend than the flammability of isopentane for reasons of being less flammable material, which is safer and easier to use. Higher LFLs allow higher concentrations in air, regardless of ignition source and potential fire or explosion.

Two aerosol cans are charged with methanol / water, one pressurized with HFC-152a and the other pressurized with an azeotropic mixture of HFC-152a and 97: 2 wt% Z-HFO-1336mzzm: ethanol. In the aerosol flame expansion test procedure, when the aerosol from the can is sprayed onto the candle and into the candle, a low flame extension is observed from the pressurized can with an azeotropic mixture of 97: 2 wt.% Z-HFO-1336mzzm: ethanol.

FLAME SUPPRESSION METHOD

The present invention also provides a method of inhibiting a print, the method comprising contacting the azeotropic composition of the present invention with a flame. If desired, additional phosphorus inhibitors may be used in the compositions of the present invention as adjuvants or as second phosphorus inhibitors. One class of compounds useful for this purpose is fluoroketones. One particularly preferred fluoro ketone is dodecafluoro-2-methylpentan-3-one. One commercial source for such a preferred compound is 3M (trade name Novec 1230).

Any suitable method of contacting the composition with a flame may be used. For example, the composition of the present invention may be sprayed, injected, etc., with a flame, or at least a portion of the flame may be absorbed into the composition.

Although the present invention has been particularly shown and described with reference to preferred embodiments thereof, those skilled in the art will readily appreciate that various changes and modifications can be made without departing from the scope of the present invention. The claims are intended to include the embodiments described, the alternatives discussed above, and all equivalents thereof.

Claims (15)

From greater than 0 to about 99% by weight of cis-1,1,1,4,4,4-hexafluoro-2-butene (Z-HFO-1336mzzm) compound; And
From about 1% to less than 100% by weight of other materials selected from the group consisting of water, fluoroketones, alcohols, hydrochlorofluoroolefins, and combinations of two or more thereof.
Azeotropic composition.
The method according to claim 1,
At least one alcohol is methanol
Azeotropic composition.
The method according to claim 1,
At least one alcohol is ethanol
Azeotropic composition.
The method according to claim 1,
From about 75% to less than 100% by weight of Z-HFO-1336mzzm and from greater than 0 to about 25% by weight of alcohol, and combinations of two or more thereof.
Azeotropic composition.
The method according to claim 1,
From about 85% to less than 100% by weight of Z-HFO-1336mzzm and from greater than 0 to about 15% by weight of alcohol, and combinations of two or more thereof.
Azeotropic composition.
The method according to claim 1,
From greater than 0 to about 50% by weight of water and from about 50% to less than 100% by weight of Z-HFO-1336mzzm
Azeotropic composition.
The method according to claim 1,
From greater than 0 to about 10% by weight of water and from about 90% to less than 100% by weight of Z-HFO-1336mzzm
Azeotropic composition.
The method according to claim 1,
From about 50% to about 99% by weight of Z-HFO-1336mzzm and from about 1% to less than 50% by weight of fluoroketone
Azeotropic composition.
The method according to claim 1,
From about 60% to about 95% by weight of Z-HFO-1336mzzm and from about 5% to less than 40% by weight of fluoroketone in an effective amount
Azeotropic composition.
The method according to claim 1,
Comprising from about 1% to about 99% Z-HFO-1336mzzm and from about 1% to about 99% trans-1,1,1-trifluoro-3-chloropropene in an effective amount
Azeotropic composition.
The method according to claim 1,
Comprising from about 90% to about 99% Z-HFO-1336mzzm and from about 1% to about 10% trans-1,1,1-trifluoro-3-chloropropene in an effective amount
Azeotropic composition.
The method according to claim 1,
An effective amount of about 4 wt% Z-HFO-1336mzzm and about 96 wt% trans-1,1,1-trifluoro-3-chloropropene
Azeotropic composition.
The method according to claim 1,
HFO-1233zd and up to about 10% Z-HFO-1336mzzm
Azeotropic composition.
A blowing agent for sprayed foams comprising the azeotropic composition of claim 1.
A refrigerant composition comprising the azeotropic composition of claim 1.

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